FIELD OF THE INVENTION
[0001] The present invention relates to golf balls. Particular example aspects of this invention
relate to golf balls having a coating that improves the aerodynamic performance of
the ball.
BACKGROUND
[0002] Golf is enjoyed by a wide variety of players - players of different genders and dramatically
different ages and/or skill levels. Golf is somewhat unique in the sporting world
in that such diverse collections of players can play together in golf events, even
in direct competition with one another (e.g., using handicapped scoring, different
tee boxes, in team formats, etc.), and still enjoy the golf outing or competition.
These factors, together with the increased availability of golf programming on television
(e.g., golf tournaments, golf news, golf history, and/or other golf programming) and
the rise of well known golf superstars, at least in part, have increased golfs popularity
in recent years, both in the United States and across the world.
[0003] Golfers at all skill levels seek to improve their performance, lower their golf scores,
and reach that next performance "level." Manufacturers of all types of golf equipment
have responded to these demands, and in recent years, the industry has witnessed dramatic
changes and improvements in golf equipment. For example, a wide range of different
golf ball models now are available, with balls designed to complement specific swing
speeds and/or other player characteristics or preferences, e.g., with some balls designed
to fly farther and/or straighter; some designed to provide higher or flatter trajectories;
some designed to provide more spin, control, and/or feel (particularly around the
greens); some designed for faster or slower swing speeds; etc. A host of swing and/or
teaching aids also are available on the market that promise to help lower one's golf
scores.
[0004] Being the sole instrument that sets a golf ball in motion during play, golf clubs
also have been the subject of much technological research and advancement in recent
years. For example, the market has seen dramatic changes and improvements in putter
designs, golf club head designs, shafts, and grips in recent years. Additionally,
other technological advancements have been made in an effort to better match the various
elements and/or characteristics of the golf club and characteristics of a golf ball
to a particular user's swing features or characteristics (e.g., club fitting technology,
ball launch angle measurement technology, ball spin rate measurement technology, ball
fitting technology, etc.).
[0005] Modem golf balls generally comprise either a one-piece construction or several layers
including an outer cover surrounding a core. Typically, one or more layers of paint
and/or other coatings are applied to the outer surface of the golf ball. For example,
in one typical design, the outer surface of the golf ball is first painted with at
least one clear or pigmented basecoat primer followed by at least one application
of a clear coating or topcoat. The clear coating may serve a variety of functions,
such as protecting the cover material (e.g., improving abrasion resistance or durability),
improving aerodynamics of ball flight, preventing yellowing, and/or improving aesthetics
of the ball.
[0006] One common coating utilizes a solvent borne two-component polyurethane, which is
applied to the exterior of a golf ball. The coating may be applied, for example, by
using compressed air to deliver and spray the coating materials.
[0007] Dimples were added to golf balls to improve the aerodynamics over smooth balls. Variations
of the dimples have been introduced over the years relating to their size, shape,
depth, and pattern. Other concepts have included the inclusion of small dimples within
dimples to provide different aerodynamic performance. Such small dimples would often
be filled up during application of a top coat to the outer surface of the ball thus
destroying the intended effect of the balls.
[0008] While the industry has witnessed dramatic changes and improvements to golf equipment
in recent years, some players continue to look for increased distance on their golf
shots, particularly on their drives or long iron shots, and/or improved spin or control
of their shots, particularly around the greens. Accordingly, there is room in the
art for further advances in golf technology.
SUMMARY
[0009] The following presents a general summary of aspects of the disclosure in order to
provide a basic understanding of the disclosure and various aspects of it. This summary
is not intended to limit the scope of the disclosure in any way, but it simply provides
a general overview and context for the more detailed description that follows.
[0010] Aspects of this invention are directed to a coating comprising a resin and particles
applied to a surface of a golf ball, as well as to golf balls including such coatings.
[0011] Other aspects of this invention are directed to methods for applying a coating comprising
a resin and particles to a surface of a golf ball.
BRIEF DESCRIPTION OF THE DRAWINGS
[0012] A more complete understanding of the present invention and certain advantages thereof
may be acquired by referring to the following detailed description in consideration
with the accompanying drawings, in which:
[0013] FIG. 1 schematically illustrates a golf ball having dimples.
[0014] FIGS. 2 and 2A schematically illustrate a cross-sectional view of a golf ball in
accordance with FIG. 1 having a coating thereon.
[0015] FIG. 3 schematically illustrates a cross-sectional view of a portion of a golf ball
having a cover layer and coating in accordance with FIG. 1 having particles contained
within a resin.
[0016] FIG. 4 schematically illustrates a cross-sectional view of a portion of a golf ball
having a cover layer and coating in accordance with FIG. 1 having particles applied
onto the surface of a resin.
[0017] FIG. 5 depicts test results for Wet Sand Abrasion.
[0018] FIG. 6 depicts test results for Wedge Abrasion.
[0019] FIG. 7 depicts spin results of golf balls with a driver.
[0020] FIG. 8 depicts spin results of golf balls with a 6 iron.
[0021] FIG. 9 depicts spin results of golf balls with a wedge.
[0022] The reader is advised that the various parts shown in these drawings are not necessarily
drawn to scale.
DETAILED DESCRIPTION
[0023] In the following description of various example structures, reference is made to
the accompanying drawings, which form a part hereof, and in which are shown by way
of illustration various example golf ball structures. Additionally, it is to be understood
that other specific arrangements of parts and structures may be utilized and structural
and functional modifications may be made without departing from the scope of the present
invention. Also, while terms such as "top," "bottom," "front," "back," "rear," "side,"
"underside," "overhead," and the like may be used in this specification to describe
various example features and elements of the invention, these terms are used herein
as a matter of convenience, e.g., based on the example orientations shown in the figures
and/or the orientations in typical use. Nothing in this specification should be construed
as requiring a specific three dimensional or spatial orientation of structures.
A. General Description of Golf Balls and Manufacturing Systems and Methods
[0024] Golf balls may be of varied construction, e.g., one-piece balls, two-piece balls,
three-piece balls (including wound balls), four-piece balls, five-piece balls, etc.
The difference in play characteristics resulting from these different types of constructions
can be quite significant. Generally, golf balls may be classified as solid or wound
balls. Solid balls that have a two-piece construction, typically a cross-linked rubber
core, e.g., polybutadiene cross-linked with zinc diacrylate and/or similar cross-linking
agents, encased by a blended cover, e.g., ionomer resins, are popular with many average
recreational golfers. The combination of the core and cover materials provide a relatively
"hard" ball that is virtually indestructible by golfers and one that imparts a high
initial velocity to the ball, resulting in improved distance. Because the materials
from which the ball is formed are very rigid, two-piece balls tend to have a hard
"feel" when struck with a club. Likewise, due to their hardness, these balls have
a relatively low spin rate, which also helps provide greater distance.
[0025] Wound balls are generally constructed from a liquid or solid center surrounded by
tensioned elastomeric material and covered with a durable cover material, e.g., ionomer
resin, or a softer cover material, e.g., balata or polyurethane. Wound balls are generally
thought of as performance golf balls and have good resiliency, desirable spin characteristics,
and good "feel" when struck by a golf club. However, wound balls are generally difficult
to manufacture as compared to solid golf balls.
[0026] More recently, three- and four-piece balls have gained popularity, both as balls
for average recreational golfers as well as performance balls for professional and
other elite level players. Such balls typically include a core (optionally a multipart
core, such as an inner core and an outer core), one or more mantle or intermediate
layers (also called "inner cover" layers), and an outer cover layer.
[0027] A variety of golf balls have been designed to provide particular playing characteristics.
These characteristics generally include the initial velocity and spin of the golf
ball, which can be optimized for various types of players. For instance, certain players
prefer a ball that has a high spin rate in order to control and stop the golf ball
around the greens. Other players prefer a ball that has a low spin rate and high resiliency
to maximize distance. Generally, a golf ball having a hard core and a soft cover will
have a high spin rate. Conversely, a golf ball having a hard cover and a soft core
will have a low spin rate. Golf balls having a hard core and a hard cover generally
have very high resiliency for distance, but they may "feel" hard and be difficult
to control around the greens.
[0028] The carry distance of some conventional two-piece balls has been improved by altering
the typical single layer core and single cover layer construction to provide a multi-layer
ball, e.g., a dual cover layer, dual core layer, and/or a ball having an intermediate
layer disposed between the cover and the core. Three- and four-piece balls are now
commonly found and commercially available. Aspects of this invention may be applied
to all types of ball constructions, including the wound, solid, and/or multi-layer
ball constructions described above.
[0029] FIG. 1 shows an example of a golf ball 10 that includes a plurality of dimples 18
formed on its outer surface. FIGS. 2 and 2A show an example of a golf ball 10, which
has a core 12, an intermediate layer 14, a cover 16 having a plurality of dimples
18 formed therein, and a coating 20 applied over the exterior surface of the golf
ball 10. The golf ball 10 alternatively may be only one piece such that the core 12
represents the entirety of the golf ball 10, and the plurality of dimples are formed
on the core 12. The ball 10 also may have any other desired construction, including
conventional constructions and the various example constructions described herein.
The thickness of the coating 20 typically is significantly less than that of the cover
16 or the intermediate layer 14, and by way of example may range from about 8 to about
50 µm. The coating 20 should be substantially uniformly applied to the exterior of
the ball (e.g., a substantially uniform thickness) and should have a minimal effect
on the depth and volume of the dimples 18. An optional primer or basecoat may be applied
to the exterior surface of the cover 16 of the golf ball 10 prior to application of
the coating layer 20.
The Center
[0030] A golf ball may be formed, for example, with a center having a low compression, but
still exhibit a finished ball COR and initial velocity approaching that of conventional
two-piece distance balls. The center may have, for example, a compression of about
60 or less. The finished balls made with such centers have a COR, measured at an inbound
speed of 125 ft./s., of about 0.795 to about 0.815. "COR" refers to Coefficient of
Restitution, which is obtained by dividing a ball's rebound velocity by its initial
(i.e., incoming) velocity. This test is performed by firing the samples out of an
air cannon at a vertical steel plate over a range of test velocities (e.g., from 75
to 150 ft/s). A golf ball having a high COR dissipates a smaller fraction of its total
energy when colliding with the plate and rebounding therefrom than does a ball with
a lower COR.
[0031] The terms "points" and "compression points" refer to the compression scale or the
compression scale based on the ATTI Engineering Compression Tester. This scale, which
is well known to persons skilled in the art, is used in determining the relative compression
of a center or ball.
[0032] The center may have, for example, a Shore C hardness of about 40 to about 80. The
center may have a diameter of about 0.75 inches to about 1.68 inches. The base composition
for forming the center may include, for example, polybutadiene and about 20 to 50
parts of a metal salt diacrylate, dimethacrylate, or monomethacrylate. If desired,
the polybutadiene can also be mixed with other elastomers known in the art, such as
natural rubber, styrene butadiene, and/or isoprene, in order to further modify the
properties of the center. When a mixture of elastomers is used, the amounts of other
constituents in the center composition are usually based on 100 parts by weight of
the total elastomer mixture. In other examples, the center (or core) may be made from
resin materials, such as HPF resins (optionally with barium sulfate included therein),
which are commercially available from E.I. DuPont de Nemours and Company of Wilmington,
Delaware.
[0033] Metal salt diacrylates, dimethacrylates, and monomethacrylates include without limitation
those wherein the metal is magnesium, calcium, zinc, aluminum, sodium, lithium or
nickel. Zinc diacrylate, for example, provides golf balls with a high initial velocity
in the United States Golf Association ("USGA") test.
[0034] Free radical initiators often are used to promote cross-linking of the metal salt
diacrylate, dimethacrylate, or monomethacrylate and the polybutadiene. Suitable free
radical initiators include, but are not limited to peroxide compounds, such as dicumyl
peroxide; 1,1-di(t-butylperoxy) 3,3,5-trimethyl cyclohexane; bis (t-butylperoxy) diisopropylbenzene;
2,5-dimethyl-2,5 di (t-butylperoxy) hexane; or di-t-butyl peroxide; and mixtures thereof.
The initiator(s) at 100 percent activity may be added in an amount ranging from about
0.05 to about 2.5 pph based upon 100 parts of butadiene, or butadiene mixed with one
or more other elastomers. Often the amount of initiator added ranges from about 0.15
to about 2 pph, and more often from about 0.25 to about 1.5 pph. The golf ball centers
may incorporate 5 to 50 pph of zinc oxide (ZnO) in a zinc diacrylate-peroxide cure
system that cross-links polybutadiene during the core molding process.
[0035] The center compositions may also include fillers, added to the elastomeric (or other)
composition to adjust the density and/or specific gravity of the center. Non-limiting
examples of fillers include zinc oxide, barium sulfate, and regrind, e.g., recycled
core molding matrix ground to about 30 mesh particle size. The amount and type of
filler utilized is governed by the amount and weight of other ingredients in the composition,
bearing in mind a maximum golf ball weight of 1.620 oz has been established by the
USGA. Fillers usually range in specific gravity from about 2.0 to about 5.6. The amount
of filler in the center may be lower such that the specific gravity of the center
is decreased.
[0036] The specific gravity of the center may range, for example, from about 0.8 to about
1.3, depending upon such factors as the size of the center, cover, intermediate layer
and finished ball, as well as the specific gravity of the cover and intermediate layer.
Other components such as accelerators, e.g., tetra methylthiuram, processing aids,
processing oils, plasticizers, dyes and pigments, antioxidants, as well as other additives
well known to the skilled artisan may also be used in amounts sufficient to achieve
the purpose for which they are typically used.
Intermediate Layer(s)
[0037] The golf ball also may have one or more intermediate layers formed, for example,
from dynamically vulcanized thermoplastic elastomers, functionalized styrene-butadiene
elastomers, thermoplastic rubbers, polybutadiene rubbers, natural rubbers, thermoset
elastomers, thermoplastic urethanes, metallocene polymers, thermoset urethanes, ionomer
resins, or blends thereof. For example, an intermediate layer may include a thermoplastic
or thermoset polyurethane. Non-limiting of commercially available dynamically vulcanized
thermoplastic elastomers include SANTOPRENE
®, SARLINK
®, VYRAM
®, DYTRON
®, and VISTAFLEX
® SANTOPRENENR
® is a dynamically vulcanized PP/EPDM. Examples of functionalized styrene-butadiene
elastomers, i.e., styrene-butadiene elastomers with functional groups such as maleic
anhydride or sulfonic acid, include KRATON FG-1901x and FG-1921x, which are available
from the Shell Corporation of Houston, Tex.
[0038] Examples of suitable thermoplastic polyurethanes include ESTANE
® 58133, ESTANE
® 58134 and ESTANE
® 58144, which are commercially available from the B. F. Goodrich Company of Cleveland,
Ohio.
[0039] Examples of metallocene polymers, i.e., polymers formed with a metallocene catalyst,
include those commercially available from Sentinel Products of Hyannis, Mass. Suitable
thermoplastic polyesters include polybutylene terephthalate.
Thermoplastic ionomer resins may be obtained by providing a cross metallic bond to
polymers of monoolefin with at least one member selected from the group consisting
of unsaturated mono- or di-carboxylic acids having 3 to 12 carbon atoms and esters
thereof (the polymer contains 1 to 50 percent by weight of the unsaturated mono- or
di-carboxylic acid and/or ester thereof). More particularly, low modulus ionomers
such as acid-containing ethylene copolymer ionomers, include E/X/Y copolymers where
E is ethylene, X is a softening comonomer such as acrylate or methacrylate. Non-limiting
examples of ionomer resins include SURLYN
® and IOTEK®, which are commercially available from DuPont and Exxon, respectively.
[0040] Alternatively, the intermediate layer(s) may be a blend of a first and a second component
wherein the first component is a dynamically vulcanized thermoplastic elastomer, a
functionalized styrene-butadiene elastomer, a thermoplastic or thermoset polyurethane
or a metallocene polymer and the second component is a material such as a thermoplastic
or thermoset polyurethane, a thermoplastic polyetherester or polyetheramide, a thermoplastic
ionomer resin, a thermoplastic polyester, another dynamically vulcanized elastomer,
another a functionalized styrene-butadiene elastomer, another a metallocene polymer
or blends thereof. At least one of the first and second components may include a thermoplastic
or thermoset polyurethane.
[0041] One or more intermediate layers also may be formed from a blend containing an ethylene
methacrylic/acrylic acid copolymer. Non-limiting examples of acid-containing ethylene
copolymers include ethylene/acrylic acid; ethylene/methacrylic acid; ethylene/acrylic
acid/n- or isobutyl acrylate; ethylene/methacrylic acid/n- or iso-butyl acrylate;
ethylene/acrylic acid/methyl acrylate; ethylene/methacrylic acid/methyl acrylate;
ethylene/acrylic acid/isobornyl acrylate or methacrylate and ethylene/methacrylic
acid/isobornyl acrylate or methacrylate. Examples of commercially available ethylene
methacrylic/acrylic acid copolymers include NUCREL
® polymers, available from DuPont.
[0042] Alternatively, the intermediate layer(s) may be formed from a blend which includes
an ethylene methacrylic/acrylic acid copolymer and a second component which includes
a thermoplastic material. Suitable thermoplastic materials for use in the intermediate
blend include, but are not limited to, polyesterester block copolymers, polyetherester
block copolymers, polyetheramide block copolymers, ionomer resins, dynamically vulcanized
thermoplastic elastomers, styrene-butadiene elastomers with functional groups such
as maleic anhydride or sulfonic acid attached, thermoplastic polyurethanes, thermoplastic
polyesters, metallocene polymers, and/or blends thereof.
[0043] An intermediate layer often has a specific gravity of about 0.8 or more. In some
examples the intermediate layer has a specific gravity greater than 1.0, e.g., ranging
from about 1.02 to about 1.3. Specific gravity of the intermediate layer may be adjusted,
for example, by adding a filler such as barium sulfate, zinc oxide, titanium dioxide
and combinations thereof.
[0044] The intermediate layer blend may have a flexural modulus of less than about 10,000
psi, often from about 5,000 to about 8,000 psi. The intermediate layers often have
a Shore D hardness of about 35 to 70. The intermediate layer and core construction
together may have a compression of less than about 65, often from about 50 to about
65. Usually, the intermediate layer has a thickness from about 0.020 inches to about
0.2 inches. The golf balls may include a single intermediate layer or a plurality
of intermediate layers. In the case where a ball includes a plurality of intermediate
layers, a first intermediate layer outside the core may include, for example, a thermoplastic
material or a rubber material (synthetic or natural) having a hardness greater than
that of the core. A second intermediate layer may be disposed around the first intermediate
layer and may have a greater hardness than that of the first intermediate layer. The
second intermediate layer may be formed of materials such as polyether or polyester
thermoplastic urethanes, thermoset urethanes, and ionomers such as acid-containing
ethylene copolymer ionomers.
[0045] In addition, if desired, a third intermediate layer (or even more layers) may be
disposed in between the first and second intermediate layers. The third intermediate
layer may be formed of the variety of materials as discussed above. For example, the
third intermediate layer may have a hardness greater than that of the first intermediate
layer.
The Cover Layer
[0046] A golf ball also typically has a cover layer that includes one or more layers of
a thermoplastic or thermosetting material. A variety of materials may be used such
as ionomer resins, thermoplastic polyurethanes, balata and blends thereof.
[0047] The cover may be formed of a composition including very low modulus ionomers (VLMIs).
As used herein, the term "very low modulus ionomers," or the acronym "VLMIs," are
those ionomer resins further including a softening comonomer X, commonly a (meth)acrylate
ester, present from about 10 weight percent to about 50 weight percent in the polymer.
VLMIs are copolymers of an α-olefin, such as ethylene, a softening agent, such as
n-butyl-acrylate or isobutyl-acrylate, and an α, β-unsaturated carboxylic acid, such
as acrylic or methacrylic acid, where at least part of the acid groups are neutralized
by a magnesium cation. Other examples of softening comonomers include n-butyl methacrylate,
methyl acrylate, and methyl methacrylate. Generally, a VLMI has a flexural modulus
from about 2,000 psi to about 10,000 psi. VLMIs are sometimes referred to as "soft"
ionomers.
[0048] Ionomers, such as acid-containing ethylene copolymer ionomers, include E/X/Y copolymers
where E is ethylene, X is a softening comonomer such as acrylate or methacrylate present
in 0 to 50 weight percent of the polymer, and Y is acrylic or methacrylic acid present
in 5 to 35 (often 10 to 20) weight percent of the polymer, wherein the acid moiety
is neutralized 1 to 90 percent (usually at least 40 percent) to form an ionomer by
a cation such as lithium, sodium, potassium, magnesium, calcium, barium, lead, tin,
zinc or aluminum, or a combination of such cations, lithium, sodium and zinc being
the most preferred. Specific acid-containing ethylene copolymers include ethylene/acrylic
acid, ethylene/methacrylic acid, ethylene/acrylic acid/n-butyl acrylate, ethylene/methacrylic
acid/n-butyl acrylate, ethylene/methacrylic acid/iso-butyl acrylate, ethylene/acrylic
acid/iso-butyl acrylate, ethylene/methacrylic acid/n-butyl methacrylate, ethylene/acrylic
acid/methyl methacrylate, ethylene/acrylic acid/methyl acrylate, ethylene/methacrylic
acid/methyl acrylate, ethylene/methacrylic acid/methyl methacrylate, and ethylene/acrylic
acid/n-butyl methacrylate.
[0049] To aid in the processing of the cover stock, ionomer resins may be blended in order
to obtain a cover having desired characteristics. For this reason, the cover may be
formed from a blend of two or more ionomer resins. The blend may include, for example,
a very soft material and a harder material. Ionomer resins with different melt flow
indexes are often employed to obtain the desired characteristics of the cover stock.
SURLYN
® 8118, 7930 and 7940 have melt flow indices of about 1.4, 1.8, and 2.6 g/10 min.,
respectively. SURLYN
® 8269 and SURLYN
® 8265 each have a melt flow index of about 0.9 g/10 min. A blend of ionomer resins
may be used to form a cover having a melt flow index, for example, of from about 1
to about 3 g/10 min. The cover layer may have a Shore D hardness, for example, ranging
from about 45 to about 80.
[0050] The cover also may include thermoplastic and/or thermoset materials. For example,
the cover may include a thermoplastic material such as urethane or polyurethane. Polyurethane
is a product of a reaction between a polyurethane prepolymer and a curing agent. The
polyurethane prepolymer is a product formed by a reaction between a polyol and a diisocyanate.
Often, a catalyst is employed to promote the reaction between the curing agent and
the polyurethane prepolymer. In the case of cast polyurethanes, the curing agent is
typically either a diamine or glycol.
[0051] As another example, a thermoset cast polyurethane may be used. Thermoset cast polyurethanes
are generally prepared using a diisocyanate, such as 2,4-toluene diisocyanate (TDI),
methylenebis-(4-cyclohexyl isocyanate) (HMDI), or paraphenylene diisocyanate ("PPDI")
and a polyol which is cured with a polyamine, such as methylenedianiline (MDA), or
a trifunctional glycol, such as trimethylol propane, or tetrafunctional glycol, such
as N,N,N',N'-tetrakis(2-hydroxpropyl)ethylenediamine. Other suitable thermoset materials
include, but are not limited to, thermoset urethane ionomers and thermoset urethane
epoxies. Other examples of thermoset materials include polybutadiene, natural rubber,
polyisoprene, styrene-butadiene, and styrene-propylene-diene rubber.
[0052] When the cover includes more than one layer, e.g., an inner cover layer and an outer
cover layer, various constructions and materials are suitable. For example, an inner
cover layer may surround the intermediate layer with an outer cover layer disposed
thereon or an inner cover layer may surround a plurality of intermediate layers. When
using an inner and outer cover layer construction, the outer cover layer material
may be a thermoset material that includes at least one of a castable reactive liquid
material and reaction products thereof, as described above, and may have a hardness
from about 30 Shore D to about 60 Shore D.
[0053] The inner cover layer may be formed from a wide variety of hard (e.g., about 50 Shore
D or greater), high flexural modulus resilient materials, which are compatible with
the other materials used in the adjacent layers of the golf ball. The inner cover
layer material may have a flexural modulus of about 65,000 psi or greater. Suitable
inner cover layer materials include the hard, high flexural modulus ionomer resins
and blends thereof, which may be obtained by providing a cross metallic bond to polymers
of monoolefin with at least one member selected from the group consisting of unsaturated
mono- or di-carboxylic acids having 3 to 12 carbon atoms and esters thereof (the polymer
contains 1 to 50 percent by weight of the unsaturated mono- or di-carboxylic acid
and/or ester thereof). More particularly, such acid-containing ethylene copolymer
ionomer component includes E/X/Y copolymers where E is ethylene, X is a softening
comonomer such as acrylate or methacrylate present in 0-50 weight percent of the polymer,
and Y is acrylic or methacrylic acid present in 5-35 weight percent of the polymer,
wherein the acid moiety is neutralized about 1-90 percent to form an ionomer by a
cation such as lithium, sodium, potassium, magnesium, calcium, barium, lead, tin,
zinc, or aluminum, or a combination of such cations. Specific examples of acid-containing
ethylene copolymers include ethylene/acrylic acid, ethylene/methacrylic acid, ethylene/acrylic
acid/n-butyl acrylate, ethylene/methacrylic acid/n-butyl acrylate, ethylene/methacrylic
acid/iso-butyl acrylate, ethylene/acrylic acid/iso-butyl acrylate, ethylene/methacrylic
acid/n-butyl methacrylate, ethylene/acrylic acid/methyl methacrylate, ethylene/acrylic
acid/methyl acrylate, ethylene/methacrylic acid/methyl acrylate, ethylene/methacrylic
acid/methyl methacrylate, and ethylene/acrylic acid/n-butyl methacrylate.
[0054] Examples of other suitable inner cover materials include thermoplastic or thermoset
polyurethanes, polyetheresters, polyetheramides, or polyesters, dynamically vulcanized
elastomers, functionalized styrene-butadiene elastomers, metallocene polymers, polyamides
such as nylons, acrylonitrile butadiene-styrene copolymers (ABS), or blends thereof.
Manufacturing Process
[0055] While golf balls in accordance with examples of this invention may be made in any
desired manner without departing from this invention, including in conventional manners
as are known and used in the art, one common technique for manufacturing golf balls
is a laminate process. In order to form multiple layers around the center, a laminate
is first formed. The laminate includes at least two layers and sometimes includes
three layers. The laminate may be formed by mixing uncured core material to be used
for each layer and calendar rolling the material into thin sheets. Alternatively,
the laminate may be formed by mixing uncured intermediate layer material and rolling
the material into sheets. The laminate sheets may be stacked together to form a laminate
having three layers, using calender rolling mills. Alternatively, the sheets may be
formed by extrusion.
[0056] A laminate also may be formed using an adhesive between each layer of material. For
example, an epoxy resin may be used as adhesive. The adhesive should have good shear
and tensile strength, for example, a tensile strength over about 1500 psi. The adhesive
often has a Shore D hardness of less than about 60 when cured. The adhesive layer
applied to the sheets should be very thin, e.g., less than about 0.004 inches thick.
[0057] Preferably, each laminate sheet is formed to a thickness that is slightly larger
than the thickness of the layers in the finished golf ball. Each of these thicknesses
can be varied, but all have a thickness of preferably less than about 0.1 inches.
The sheets should have very uniform thicknesses.
[0058] The next step in the method is to form multiple layers around the center. This may
be accomplished by placing two laminates between a top mold and a bottom mold. The
laminates may be formed to the cavities in the mold halves. The laminates then may
be cut into patterns that, when joined, form a laminated layer around the center.
For example, the laminates may be cut into figure 8-shaped or barbell-like patterns,
similar to a baseball or a tennis ball cover. Other patterns may be used, such as
curved triangles, hemispherical cups, ovals, or other patterns that may be joined
together to form a laminated layer around the center. The patterns may then be placed
between molds and formed to the cavities in the mold halves. A vacuum source often
is used to form the laminates to the mold cavities so that uniformity in layer thickness
is maintained.
[0059] After the laminates have been formed to the cavities, the centers are then inserted
between the laminates. The laminates are then compression molded about the center
under conditions of temperature and pressure that are well known in the art. The mold
halves usually have vents to allow flowing of excess layer material from the laminates
during the compression molding process. As an alternative to compression molding,
the core and/or intermediate layer(s) may be formed by injection molding or other
suitable technique.
[0060] The next step involves forming a cover around the golf ball core. The core, including
the center and any intermediate layers, may be supported within a pair of cover mold-halves
by a plurality of retractable pins. The retractable pins may be actuated by conventional
means known to those of ordinary skill in the art.
[0061] After the mold halves are closed together with the pins supporting the core, the
cover material is injected into the mold in a liquid state through a plurality of
injection ports or gates, such as edge gates or sub-gates. With edge gates, the resultant
golf balls are all interconnected and may be removed from the mold halves together
in a large matrix. Sub-gating automatically separates the mold runner from the golf
balls during the ejection of the golf balls from mold halves.
[0062] The retractable pins may be retracted after a predetermined amount of cover material
has been injected into the mold halves to substantially surround the core. The liquid
cover material is allowed to flow and substantially fill the cavity between the core
and the mold halves, while maintaining concentricity between the core and the mold
halves. The cover material is then allowed to solidify around the core, and the golf
balls are ejected from the mold halves and subjected to finishing processes, including
coating, painting, and/or other finishing processes, including processes in accordance
with examples of this invention, as will be described in more detail below.
B. General Description of Coating Materials
[0063] The coating comprises a resin and a plurality of particles. The resin may be any
suitable resin, non-limiting examples of which include thermoplastics, thermoplastic
elastomers, such as polyurethanes, polyesters, acrylics, low acid thermoplastic ionomers,
e.g., containing up to about 15% acid, and UV curable systems.
[0064] The coating may comprise additional additives incorporated into the resin, such as
flow additives, mar/slip additives, adhesion promoters, thickeners, gloss reducers,
flexibilizers, cross-linking additives, isocyanates or other agents for toughening
or creating scratch resistance, optical brighteners, UV absorbers, and the like. The
amount of such additives usually ranges from 0 to about 5 wt%, often from 0 to about
1.5 wt%, based on total weight of the coating.
[0065] In addition, solid particles may be contained within the resin or adhered to and/or
embedded into the surface of resin as described in more detail below.
C. General Description of Coating Devices
[0066] The coating materials may be delivered by spray guns (either fixed or articulating
types). Examples of devices that may be used include heated spray equipment and electrostatic
and high volume-low pressure (HVLP) devices. The golf balls are typically placed on
work holders, where they rotate and pass through a spray zone in a specified time
to obtain full coverage of their exterior surfaces. Additionally or alternatively,
if desired, the spray heads that apply the coating material may be movable with respect
to the balls and/or articulated to assist in applying a uniform coating to the entire
ball structure. Suitable coating systems and methods for use in this invention may
include conventional coating systems as are known and used in the art.
[0067] In some aspects of this invention, a carrier fluid comprising nitrogen gas or nitrogen-enriched
air may be used to deliver the coating material to the exterior surface of the golf
ball. Nitrogen is clean, dry (anhydrous) in its elemental gas state. Nitrogen can
be ionized to eliminate problems associated with moisture and static electricity.
[0068] Suitable equipment for applying coatings using nitrogen-enriched air is described,
for example, in
U.S. Patent 6,821,315, the disclosure of which is incorporated by reference in its entirety. Such devices
are commercially available from N2 Spray Solutions. In general, such devices operate
by mixing a carrier fluid under pressure and the coating material. The carrier fluid
comprises nitrogen-enriched air, which typically contains about 90-99.5% nitrogen
by volume. Nitrogen-enriched air may be produced, for example, by passing air through
hollow-fiber membranes as described in the '315 patent.
[0069] The temperature of the carrier fluid may be adjusted to optimize coating properties.
In general, heating the carrier fluid reduces viscosity and reduces the need for solvents.
Reducing viscosity improves flow, aides in atomization, and purges the solvent, resulting
in a finer spray with a higher solids content. The carrier fluid may be heated, for
example, to a temperature of about 100 to about 170 °F (38 to 76.6 °C), often from
about 150 to about 170°F (65.6 to 76.6 °C). Other parameters, such as pressure, also
may be suitably adjusted to achieve improved drying characteristics and/or other efficiencies.
For example, atomization air pressure of about 40 psi (275.8 kPa) may be employed.
U.S. Patent Appln. No. 12/470,820 filed May 22, 2009 and entitled "Method of Applying Topcoat to Exterior Surface of Golf Ball" describes
systems and methods utilizing nitrogen-containing or nitrogen-enriched delivery fluids
to apply coating materials to golf balls. This patent application is entirely incorporated
herein by reference.
D. Specific Examples of Invention
[0070] The term "golf ball body" means a golf ball before applying the top coat (e.g., core,
intermediate layers, cover layer with dimples). In terms of the discussion below,
the term "coating" often will be used to identify the top coat or last layer applied
to the golf ball, but, as also described below, if desired, another coating may be
applied over the roughened coating material, if desired, provided that an overall
roughened surface is still provided. Often the terms "paint" or "painting" are used
synonymously with a "coating" or "coating" process.
[0071] Aspects of this invention relate to golf balls having a top coat or other coating
over the cover layer, wherein this coating comprises a resin having particles contained
therein or applied thereon. The particles provide a golf ball surface having a slightly
roughened surface, as will be described in more detail below.
[0072] If the resin contains the particles, after the resin is applied to the golf ball
body to form the coating, the particles may protrude beyond an average thickness of
the resin. In some instances, the average size of the particles may be greater than
the average thickness of the resin. As shown in FIG. 3, generally the particles 22
protrude from the surface such that a thin portion of the resin 20 still covers the
particles. The surface of the ball will therefore be roughened somewhat, as shown
in FIG. 3.
[0073] If the resin itself does not contain the particles necessary to provide the roughened
surface when it is applied to the golf ball cover 18, after the resin is applied,
and prior to drying, particles may be applied to the wet resin. The particles may
adhere to and/or become embedded into the resin, but still extend from the surface
of the resin to provide a somewhat roughened surface. As shown in FIG. 4, in this
example structure and method, particles 22 are applied to the surface of resin 20.
[0074] The particles allow for fine tuning of and improvement on the aerodynamic performance
of golf balls in flight, e.g., to enable longer flights of the golf ball. The particles
cause the finish of the coating to be rougher and on a micro-scale act as small dimples,
which increase the turbulence in the air flow around the ball and reduce flow separation
on the golf ball, reducing pressure drag. Also, if desired, the durability of the
golf ball may be improved both in cut resistance and abrasion resistance, e.g., depending
on the properties of and/or materials used in the coating.
[0075] Given the general description of various example aspects of the invention provided
above, more detailed descriptions of various specific examples of golf ball structures
according to the invention are provided below.
II. Detailed Description of Example Golf Balls, and Methods According to Aspects of
the Invention
[0076] The following discussion and accompanying figures describe various example golf balls
in accordance with aspects of the present invention. When the same reference number
appears in more than one drawing, that reference number is used consistently in this
specification and the drawings to refer to the same or similar parts throughout.
[0077] FIG. 3 and FIG. 4 demonstrate aspects of the invention related to golf balls having
a top coat or other coating comprising resin and particles contained within the resin
or applied and/or embedded thereon, respectively.
[0078] The particles may be of any shape and may be regular, irregular, uniform, nonuniform,
or mixtures thereof. The particles may be any polygon or geometric shape, including
regular shapes, such as spheres or cubes. The spheres may have a round cross-section
or may be flattened to provide an elongated or oval cross-section. The cubes may be
of square or rectangular cross-section. Irregular shapes may be defined by an irregular
surface, an irregular perimeter, protrusions, or extensions. The particles may be
rounded, elongated, smooth, rough, or have edges. Combinations of different shapes
of particles may be used. Crystalline or regular particles such as tetrapods may also
be used.
[0079] Particles may be made from any material known in the art, such as organic or inorganic,
plastics, composite materials, and metals. Suitable particles include, but are not
limited to amorphous particles such as silicas and crystalline particles such as metal
oxides, e.g., zinc oxide, iron oxides, or titanium oxide. As additional examples,
particles may comprise fumed silica, amorphous silica, colloidal silica, alumina,
colloidal alumina, titanium oxide, cesium oxide, yttrium oxide, colloidal yttria,
zirconia, colloidal zirconia, polyethylene terephthalate, polybutylene terephthalate,
polyethylene naphthalate, vinyl esters, epoxy materials, phenolics, aminoplasts, polyurethanes
and composite particles of silicon carbide or aluminum nitride coated with silica
or carbonate.
[0080] The particles may be selected to fine-tune the roughness of the golf ball to achieve
the desired aerodynamic qualities of the golf ball as well as to improve abrasion
resistance. The particles may by of any suitable hardness and durability. Softer particles
tend to affect spin, for example.
[0081] The average size of the particles depends on the material selected for the particles.
Generally, the particle sizes will range from 400 nm to 40 microns, and in some example
constructions, from 5 to 20 microns. In one particular example, the particle sizes
range from 8 to 12 microns. The particles may be approximately the same size or may
be different sizes within the defined ranges. If the particles are applied to the
surface of the resin, they would generally be smaller than if they were contained
within the coating.
[0082] Any suitable resin may be used including thermoplastics, thermoplastic elastomers
such as polyurethanes, polyesters, acrylics, low acid thermoplastic ionomers, e.g.,
containing up to about 15% acid, and UV curable systems. Specific examples include
AKZO NOBEL 7000A103.
[0083] Additional additives optionally may be incorporated into the resin, such as flow
additives, mar/slip additives, adhesion promoters, thickeners, gloss reducers, flexibilizers,
cross-linking additives, isocyanates or other agents for toughening or creating scratch
resistance, optical brighteners, UV absorbers, and the like. The amount of such additives
usually ranges from 0 to about 5 wt%, often from 0 to about 1.5 wt%.
[0084] The viscosity of the resin prior to application to the golf ball body is generally
16 to 24 seconds as measured by #2 Zahn cup. Generally the resin is thin enough to
easily spray the coating onto the golf ball body, but thick enough to prevent the
resin from substantially running after application to the golf ball body.
[0085] The thickness of the applied resin (after drying) typically ranges from of about
8 to about 50 µm, and in some examples, from about 10 to about 15 µm. When the particles
are contained within the resin, the thickness of the resin may be less than the particle
size in order to allow the particles to protrude from the resin.
[0086] The coating contains a plurality of particles, generally, 0.1 to 30 wt% particles
based on total coating weight, for example, 3 to 10 wt%.
[0087] The coating may be clear or opaque and may be white or have a tint or hue. The particles
may be of any color. Generally application of the coating and particles to the outside
of the golf ball will give the ball somewhat of a dull or matte finish, as compared
to the brighter or shinier finish of many conventional golf balls. The particles tend
to diffuse some of the light in a clear coat for example.
[0088] According to the one aspect of the present invention, a coating is formed by applying
and drying a resin on the surface of the golf ball body. The method of applying the
resin is not limited. For example, a two-component curing type resin such as a polyurethane
may be applied by an electrostatic coating method, or spray method using a spray gun,
for example after mixing an aqueous polyol liquid with a polyisocyanate. In the case
of applying the coating with the spray gun, the aqueous polyol liquid and the polyisocyanate
may be mixed bit by bit, or the aqueous polyol liquid and the polyisocyanate are fed
with the respective pumps and continuously mixed in a constant ratio through the static
mixer located in the stream line just before the spray gun. Alternatively, the aqueous
polyol liquid and the polyisocyanate can be air-sprayed respectively with the spray
gun having the device for controlling the mixing ratio thereof. Subsequently, the
two-component curing type urethane resin on the surface of the golf ball body is dried.
[0089] In one aspect the coating comprises resin (with any additives) and particles mixed
therein. The coating is applied to the golf ball body such as described above. Prior
to application to the golf ball body, the particles may be added to the resin as a
separate ingredient, or may be pre-mixed with one of the components in a two-component
coating composition.
[0090] In another aspect, a resin layer (with any additives) is applied to the golf ball
body such as described above. Prior to drying, particles are applied to the top of
the wet resin layer using a media blaster, sand blaster, powder coating device, or
other suitable device. The particles may adhere to the surface and/or be embedded
into the surface of the resin layer.
[0091] In another aspect, a very thin resin layer may be applied on top of the particles
to hold the particles in place. Generally this resin layer is composed of the same
resin layer initially applied, but may have a thinner viscosity. This additional thin
layer of resin may be provided, if necessary or desired, to fine tune or somewhat
reduce the exterior surface roughness of the ball.
Examples
[0092] Golf balls were prepared with the following coatings and then tested for various
properties
Inventive #1 - Polyurethane Clear Coat with small silica particles (1 um to 500 nm).
Smooth appearance.
Inventive #2 - Polyurethane Clear Coat with large silica particles (1 um to 5 um).
Rough, matte appearance.
Comparative -Standard Polyurethane Clear Coat with no particles.
[0093] In the Wet Sand Abrasion test, balls were tumbled in wet sand for 8 hrs. The balls
were compared visually. Lower scores indicated less damage to the ball. The balls
were graded from 1 to 5 with 1 being the best and 5 being the worst. Attention is
drawn to Fig. 5.
[0094] In the Wedge Abrasion test, balls were hit with a standard 56 deg. wedge and the
degree of scuffing was visually analyzed. Lower scores again indicated less damage
to the ball. The balls were graded from 1 to 5 with 1 being the best and 5 being the
worst. Attention is drawn to Fig. 6.
[0095] The spin graphs (Figs. 7-9) show the inventive coating can increase spin off of irons
and wedges without increasing driver spin. This is advantageous for more distance
off the drive (lower spin) and more control around the green (higher spin).
[0096] The golf ball body of the present invention has no limitation on its structure and
includes a one-piece golf ball, a two-piece golf ball, a multi-piece golf ball comprising
at least three layers, and a wound-core golf ball. The present invention can be applied
for all types of the golf ball.
III. Conclusion
[0097] The present invention is described above and in the accompanying drawings with reference
to a variety of example structures, features, elements, and combinations of structures,
features, and elements. The purpose served by the disclosure, however, is to provide
examples of the various features and concepts related to the invention, not to limit
the scope of the invention. One skilled in the relevant art will recognize that numerous
variations and modifications may be made to the embodiments described above without
departing from the scope of the present invention, as defined by the appended claims.
For example, the various features and concepts described above in conjunction with
the figures may be used individually and/or in any combination or subcombination without
departing from this invention.
Clauses:
[0098]
- 1. A golf ball, comprising:
a golf ball body having an outer surface including a plurality of dimples formed therein;
and
a coating applied to the outer surface of the golf ball body;
the coating comprising a resin and a plurality of particles, wherein the particles
have an average size of 400 nm to 40 microns.
- 2. The golf ball according to clause I wherein the particles have an average size
of 5 to 20 microns.
- 3. The golf ball according to clause I wherein the resin has an average thickness
of 8 to 50 microns.
- 4. The golf ball according to clause 1 wherein the resin has an average thickness
of 10 to 15 microns.
- 5. The golf ball of clause 1 wherein the resin includes a thermoplastic elastomer.
- 6. The golf ball of clause 5 wherein the thermoplastic elastomer is selected from
the group consisting of polyurethanes, polyesters, acrylics, and low acid thermoplastic
ionomers containing up to about 15% acid.
- 7. The golf ball of clause 1 wherein the resin is UV curable.
- 8. The golf ball of clause 1 wherein the coating further comprises up to about 5 wt%
of at least one component selected from the group consisting of: flow additives, mar/slip
additives, adhesion promoters, thickeners, gloss reducers, flexibilizers, cross-linking
additives, isocyanates, optical brighteners, and UV absorbers, based on a total weight
of the coating.
- 9. The golf ball of clause I wherein the particles comprise 1 to 30 wt% of the total
weight of the coating.
- 10. The golf ball of clause 1 wherein the particles are selected from the group consisting
of: fumed silica, amorphous silica, colloidal silica, alumina, colloidal alumina,
titanium oxide, cesium oxide, yttrium oxide, colloidal yttria, zirconia, colloidal
zirconia, polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate,
vinyl esters, epoxy materials, phenolics, aminoplasts, polyurethanes and composite
particles of silicon carbide or aluminum nitride coated with silica or carbonate.
- 11. The golf ball according to clause 1 wherein the coating comprises particles contained
within the resin.
- 12. The golf ball according to clause 1 wherein the coating comprises a resin layer
applied to the outer surface of the golf ball body and a plurality of particles adhered
to or embedded in an outer surface of the resin layer.
- 13. The golf ball according to clause 1 wherein the golf ball body comprises a core
and a cover layer, wherein the plurality of dimples are formed in the cover layer.
- 14. A method of forming a coating on an outer surface of a golf ball body comprising:
- a) combining a resin and a plurality of particles;
- b) applying the combination of resin and particles to the outer surface of the golf
ball body, wherein the outer surface of the golf ball body includes a plurality of
dimples formed therein;
wherein the particles have an average particle size of 400 nm to 40 microns.
- 15. the method of clause 14 wherein the combination of resin and particles is applied
by spraying.
- 16. the method according to clause 14 wherein the particles have an average size of
5 to 20 microns
- 17. The method according to clause 14 further wherein the resin applied to the golf
ball body has an average thickness of 8 to 50 microns.
- 18. The method according to clause 14 wherein the resin applied to the golf ball body
has an average thickness of 10 to 15 microns.
- 19. A method of forming a coating on an outer surface of a golf ball body comprising:
- a) applying a resin layer to the outer surface of the golf ball body, wherein the
outer surface of the golf ball body includes a plurality of dimples formed therein;
- b) applying a plurality of partieles to an exterior surface of the resin layer, wherein
the particles are adhered to or embedded into the surface of the resin layer;
wherein the particles have an average particle size of 400 nm to 40 microns.
- 20. The method of clause 19 wherein the combination of resin and particles is applied
by spraying.
- 21. The method according to clause 19 wherein the particles have an average size of
5 to 20 microns.
- 22. The method according to clause 19 further wherein the resin applied to the golf
ball body has an average thickness of 8 to 50 microns.
- 23. The method according to clause 19 wherein the resin applied to the golf ball body
has an average thickness of 10 to 15 microns.